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40220-08-4

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  • 2-Propenoic acid,1,1',1''-[(2,4,6-trioxo-1,3,5-triazine-1,3,5(2H,4H,6H)-triyl)tri-2,1-ethanediyl]ester Manufacturer/High quality/Best price/In stock

    Cas No: 40220-08-4

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40220-08-4 Usage

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 40220-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,2 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40220-08:
(7*4)+(6*0)+(5*2)+(4*2)+(3*0)+(2*0)+(1*8)=54
54 % 10 = 4
So 40220-08-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H21N3O9/c1-4-13(22)28-10-7-19-16(25)20(8-11-29-14(23)5-2)18(27)21(17(19)26)9-12-30-15(24)6-3/h4-6H,1-3,7-12H2

40220-08-4 Well-known Company Product Price

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  • Aldrich

  • (407534)  Tris[2-(acryloyloxy)ethyl]isocyanurate  

  • 40220-08-4

  • 407534-250G

  • 1,216.80CNY

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40220-08-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Isocyanuric Acid Tris(2-Acryloyloxyethyl) Ester

1.2 Other means of identification

Product number -
Other names Isocyanuric Acid Tris(2-acryloyloxyethyl) Ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Adhesives and sealant chemicals,Photosensitive chemicals
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:40220-08-4 SDS

40220-08-4Downstream Products

40220-08-4Relevant articles and documents

A three-(2 - hydroxyethyl) isocyanuric acid and acrylic acid ester mixture preparation method

-

Paragraph 0108-0118, (2017/04/29)

The invention discloses a preparation method of a tri(2-ethoxy) isocyanurate acrylate mixture and belongs to the chemical engineering field. The method comprises the following steps: adding a reaction material into a reactor and uniformly mixing; heating a reaction system to 80-100 DEG C and maintaining for 4-8 hours, after reaction, cooling and washing, then standing for layering, and taking an upper organic phase; adding a polymerization inhibitor into the organic phase and decompressing and distilling to remove a solvent in the organic phase; and pressurizing and filtering the organic phase to obtain the tri(2-ethoxy) isocyanurate acrylate mixture. According to the preparation method disclosed by the invention, the reaction temperature is 80-100 DEG C, and impurities in the reaction system are removed by washing for 3-5 times; the solvent is separated from the reaction system by decompression and distillation, and pressurization and filtration are carried out to obtain a pure mixture. The mixture is simple in preparation step, relatively low in cost and can be industrially produced on a large scale; meanwhile, the proportion of tri(2-ethoxy) isocyanurate diacrylate and tri(2-ethoxy) isocyanurate triacrylate can be tracked, and the reaction is finished in any proportion to obtain mixtures with different chemical properties.

New selective syntheses of (Meth)acrylic monomers: Isocyanates, isocyanurates, carbamates and ureas derivatives

Dubosclard-Gottardi, Christine,Caubere, Paul,Fort, Yves

, p. 2561 - 2572 (2007/10/02)

The selective formulation of ω-isocyanatoalkyl (meth)acrylates may be conveniently obtained by simple condensation of potassium cyanate with ω-halogeno-alkyl (meth)acrylates under appropriated phase transfer catalytic conditions. Depending on the reaction media and the temperature, these isocyanate derivatives may be isolated, trimerized to the corresponding isocyanurates or trapped in situ as carbamates or ureas compounds.

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